510(k) · Cleared
ClearedPalm Pro Premium, Model 6PF1 & Palm Pro, Model 6PF2, Latex Exam Glove
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Dipped Products (Thailand), Ltd. · LYY Latex Patient Examination Glove
Cleared on Feb 7, 2005 as substantially equivalent to K012815 (Kimberly-Clark Corp., 2001) and 1 other predicate after a 14-day review. Its family tree reaches back 1 generation to 1993.
- Decided
- Feb 7, 2005
- Review
- 14 days
- Class
- Class I
- Product code
- LYY
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 1 generation to K913766 (1993). 2 ancestors in all. No later device cites it as a predicate yet.
- Root · 1 generation backK913766 Ansell NO Powder Ambi Patient Examination GlovesAnsell, Inc. · 1993
- This deviceK050152 Palm Pro Premium, Model 6PF1 & Palm Pro, Model 6PF2, Latex Exam GloveDipped Products (Thailand), Ltd. · 2005
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K913766 | Ansell NO Powder Ambi Patient Examination Gloves | Ansell, Inc. | 1993 | — |
| 0 (this device) | K050152 | Palm Pro Premium, Model 6PF1 & Palm Pro, Model 6PF2, Latex Exam Glove | Dipped Products (Thailand), Ltd. | 2005 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2001 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in LYY? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new LYY device
- #1 K202377 Palm Care Latex Examination Powder Free Glovesscore 12.7 · 2 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K012815 | Safeskin Healthtouch Powder-Free Exam Glove with Vitamin E and AloeSummary page 1…xamination Gloves With Protein Content Labeling Claim (50 Micrograms or Less) Predicate Device: Kimberly Clark Saleskin product, K012815 Ansell Protective Products Accutech Ambi 91-109 product K913766 Descr… | 2001 |
| * | K913766 | Ansell NO Powder Ambi Patient Examination GlovesSummary page 1…vice: Kimberly Clark Saleskin product, K012815 Ansell Protective Products Accutech Ambi 91-109 product K913766 Description of Device: A non-sterile, disposable, patient examination glove made of… | 1993 |
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- None of the 2 ancestors has a recall.
How does its category compare?
All LYY devicesLYY Latex Patient Examination Glove: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · LYY
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · LYY
150in 2022
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LYY
1in 2020
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · LYY
1in 2025
MAUDE reports naming product code LYY, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 12 | 75 | 0 | 11 |
| 2008 | 13 | 151 | 0 | 14 |
| 2009 | 7 | 76 | 0 | 11 |
| 2010 | 13 | 106 | 0 | 10 |
| 2011 | 11 | 127 | 1 | 4 |
| 2012 | 11 | 133 | 0 | 1 |
| 2013 | 6 | 131 | 0 | 2 |
| 2014 | 3 | 156 | 0 | 6 |
| 2015 | 3 | 251 | 0 | 5 |
| 2016 | 4 | 142 | 0 | 7 |
| 2017 | 4 | 230 | 0 | 7 |
| 2018 | 2 | — | 0 | 0 |
| 2019 | 1 | — | 0 | 7 |
| 2020 | 1 | — | 1 | 1 |
| 2021 | 8 | 188 | 0 | 1 |
| 2022 | 14 | 150 | 0 | 0 |
| 2023 | 2 | — | 0 | 0 |
| 2024 | 1 | — | 0 | 6 |
| 2025 | 1 | — | 0 | 1 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
A powder-free patient examination glove is a disposable device made of natural rubber latex material that may bear a trace amount of glove powder and is intended to be worn on the hand or finger(s) for medical purposes to provide a barrier against potentially infectious materials and other contaminants.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K050152 · printed Nov 4, 2026
Cite this page
510(k) Report. “K050152: Palm Pro Premium, Model 6PF1 & Palm Pro, Model 6PF2, Latex Exam Glove.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K050152
Report an extraction error
Are you the manufacturer?
Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026